|Publication number||US4657564 A|
|Application number||US 06/808,784|
|Publication date||Apr 14, 1987|
|Filing date||Dec 13, 1985|
|Priority date||Dec 13, 1985|
|Also published as||CA1320804C, DE3678402D1, EP0226141A2, EP0226141A3, EP0226141B1|
|Publication number||06808784, 808784, US 4657564 A, US 4657564A, US-A-4657564, US4657564 A, US4657564A|
|Original Assignee||Air Products And Chemicals, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (18), Non-Patent Citations (2), Referenced by (39), Classifications (23), Legal Events (6)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The present invention relates to polymeric membranes which are used to separate components of a gas mixture. It also relates to gas separation processes using the polymeric membranes.
A review of emerging technology using membranes to separate acid gases such as CO2, H2 S and SO2 from gas streams is disclosed by S. Kulkarni, et al. in an article entitled, "Membrane Separation Processes for Acid Gases," AIChE Symposium Series (1983). Both currently available and potential polymer membranes for the separation of CO2 from natural gas are disclosed. The permeation characteristics of various types of membranes, such as asymmetric cellulose esters, multi-component polysulfone/silicon rubber, ultrathin polyetherimide, and ultrathin silicone rubber/polycarbonate, were calculated for CO2 /CH4 gas mixtures.
U.S. Pat. No. 4,486,202 discloses gas separation membranes exhibiting improved gas separation selectivity. A preformed, asymmetrical gas separation membrane having selective permeation of at least one gas in a gaseous mixture over that of one or more remaining gases in the gaseous mixture, is contacted on one or both sides with a Lewis acid. Contacting the asymmetrical membrane with a Lewis acid results in improved separation factors for the permeating gases. The patent also discloses a method for producing improved, asymmetrical membranes in flat film or hollow fiber form having improved gas separation properties by treatment with a volatile Lewis acid.
U.S. Pat. No. 4,472,175 discloses gas separation membranes exhibiting improved gas separation selectivity. In this patent, a preformed, asymmetrical gas separation membrane, having selective permeation for at least one gas in a gaseous mixture over that of one or more remaining gases in a gaseous mixture, is contacted on one or both sides with a Bronsted-Lowry acid. Contacting the asymmetrical membrane with a Bronsted-Lowry acid results in improved separation factors for the permeating gases. Additionally, this patent discloses a method for producing improved, asymmetric membranes in flat film or hollow fiber form having improved gas separation properties by treatment with a Bronsted-Lowry acid.
U.K. patent application No. 2135319A discloses a membrane having improved permeability for a variety of gases. The membrane is formed from a polymer having repeating units of the formula: ##STR3## wherein R is an alkyl radical having 1-12 carbon atoms. The polymer is dissolved in one or more solvents, such as aliphatic hydrocarbons, to form a polymer solution which is cast to form a film. The membranes may be produced in any form, such as plain film, tubular and hollow fibrous forms and, if necessary, may be supported on one or more backing layers to form composites.
U.S. Pat. No. 4,020,223 discloses a method of modifying the surface of synthetic resins selected from the group consisting of polyolefins and polyacrylonitriles by treatment with a fluorine-containing gas. The fluorinated resin fibers exhibit good soil release and good water adsorption or moisture transport properties.
The present invention is a treated, semi-permeable, polymeric membrane having improved selectivity for use in separating components of a feed gas mixture. The membrane is a polymer, cast into membrane form, having the general structural formula: ##STR4## Wherein R1 is a linear or branched C1 -C4 alkyl group; R2 and R3 are independently linear or branched C1 -C6 alkyl groups; R4 is a linear or branched C1 -C12 alkyl or aryl group; X is a C1 -C3 alkyl group or ##STR5## m is at least 100; and n is 0 or 1, which has been treated by contacting it with a reactive source of fluorine for a time sufficient to modify the membrane such that the O2 /N2 selectivity ratio of the membrane is increased by at least 50% over that of the membrane prior to contact with the reactive fluorine source.
The present treated; i.e., fluorinated, polymeric membrane exhibits good gas permeability properties with a significant increase in gas selectivity over the unfluorinated polymer. Increased selectivity of the membrane is achieved for a wide variety of gas streams which contain at least two components having different permeability rates through the membrane.
The present invention is also a process for separating feed gas mixtures containing at least two components having different permeabilities through the membrane, by bringing said feed gas mixture into contact with a treated, semi-permeable, polymeric membrane as described above.
The present invention is a treated, semi-permeable, polymeric membrane which exhibits both good permeability and high selectivity for a wide variety of gas mixtures. The membrane comprises a polymeric membrane which has been treated with a reactive source of fluorine to form an ultra thin, selective surface. The polymeric membrane has the general structural formula: ##STR6## wherein R1 is a linear or branched C1 -C4 alkyl group; R2 and R3 are independently linear or branched C1 -C6 alkyl groups; R4 is a linear or branched C1 -C12 alkyl or aryl group; X is a C1 -C3 alkyl group or ##STR7## m is at least 100; and n is 0 or 1.
It is expected that other Group IV A metals, such as germanium, tin and lead may be substituted for silicon in the basic polymer structure and will perform in a similar fashion as that observed for the silicon in both the base polymer and in the reaction with the reactive fluorine source to form the selective coating.
The basic polymer can be produced by any conventional polymerization method which is capable of synthesizing this type of polymer, for example, by polymerizing monomer units in an organic solvent using a suitable catalyst such as TaCl5, MoCl5, NbCl5, etc. While the polymer can have a wide range of molecular weights wherein m is at least 100, for handling and synthesis purposes it is preferred that m is less than 50,000. After it is synthesized, the polymer is cast into membrane form. The membrane form may be any conventional type of membrane, such as a flat sheet, hollow fibers or spiral wound flat sheets. In addition to self-supporting layers, the polymer may be cast onto a suitable support to form a composite structure.
The untreated polymeric membrane generally has high permeability values for a wide range of gases, but typically exhibits relatively poor gas selectivity and therefore is not suitable for many gas separation operations. To increase selectivity, after the polymer is cast into membrane form it is fluorinated by contacting it with a reactive fluorine source. One such fluorination method involves contacting the membrane with a gas stream containing between 0.01%-25% fluorine gas for a period of time between 10 seconds and 24 hours. Preferred fluorination techniques include a contact time between 0.5 and 120 minutes with a gas stream having a fluorine concentration between 0.1%-2% fluorine gas. In any case, fluorination should be sufficient to increase the O2 /N2 selectivity ratio of the membrane at ambient temperature by at least 50%. A wide variety of fluorine-containing gas streams can be used to fluorinate the film, such as F2 /O2, F2 /N2, F2 /Cl2, F2 /O2 /N2, F2 /Cl2 /N2, F2 /SO2 /N2, F2 /SO3 /N2, F2 /SO2 Cl2 /N2 and F2 /SO2 Cl/N2 etc. If a high concentration, i.e. 10%-25%, of fluorine is to be used in the fluorination step, the fluorine concentration should be incrementally staged-up slowly to avoid burning the membrane. In addition to the above-described gas-phase fluorination, other fluorination techniques can be used. For example, a liquid containing fluorinating agents may be either volatized into a reactive gas atmosphere or the membrane may be coated or dipped into a dilute solution of a fluorine containing agent followed by a gas phase volatilization. While both sides of the polymeric membrane can be subjected to the fluorine treatment, it is preferred that only one surface of the membrane be treated, thereby forming an ultra-thin selective surface only on that side of the membrane, with the remainder of the membrane consisting of the highly permeable polymeric structure.
The interaction between the silicon containing polymer and the reactive atmosphere can be carried out under ambient conditions of temperature and pressure. Alternatively, the reaction may also be performed at elevated temperatures and in the presence of a plasma field or electromagnetic radiation.
The fluorinated membrane exhibits greatly enhanced permselectivity for various gas mixtures, making it useful in many different gas separation operations. A gas stream containing two or more components is brought into contact with the membrane, and the permeate stream from the membrane is analyzed and measured to determine the permeability coefficient (P) of the various gaseous components. Permeability coefficient can be measured by the following relationship: ##EQU1## Where: J is Flux
A is Area
L is Thickness
P is Pressure
This relationship can be conveniently expressed in units of measurement termed Barrers. The relationship for Barrers is: ##EQU2##
Additionally, the permeance (P/L), as defined by Henis and Tripodi in their paper on resistence models, J. Memb. Sci. 8, 223 (1981), of the composite structure is also measured taking into account the area of the ultra thin surface layer. By comparing the permability and/or permeance values for different gaseous components, a selectivity (α) ratio for various gas mixtures can be calculated. It was found that the treated membrane structure of the present invention significantly increased the selectivity ratios of a wide number of gas mixtures. Examples of such gas mixtures include: He/CH4, He/N2, H2 /CH4, H2 /CO, H2 /N2, O2 /N2 and CO2 /CH4. While the selectivity ratios of the above gas mixtures demonstrated a significant increase, it is expected that many other gas mixtures, both binary and multi-component mixtures, would also exhibit increased selectivity ratios.
100 grams of Toluene was mixed with TaCl5 catalyst and stirred for about 5 minutes until it dissolved to form a bright yellow solution. About 25 grams of trimethyl silyl propyne (TMSP) monomer was added and the solution immediately turned dark brown. Within two hours there was a noticeable increase in solution viscosity. After 24 hours the reaction mixture was quenched in methanol, washed with about 1000 ml of methanol and then dried, leaving a PTMSP Polymer.
The polymer produced, polytrimethyl silyl propyne, (PTMSP), has the structure: ##STR8## Wherein m is at least 100.
By varying the monomer (TMPS) to catalyst (TaCl5) ratio, it was possible to control the molecular weight of the polymer. The yields and Brookfield viscosities of 1.7% toluene solutions of several of the polymers synthesized according to the above procedure are listed in Table 1 below:
TABLE 1______________________________________PHYSICAL PROPERTIES OF PTMSP RUN NUMBER 1 2 3 4______________________________________M/C.sup.(1) 25/1 100/1 100/1 200/1Yield (%) 100% 100% 100% 87%Brookfield Viscosity.sup.(2) 164 248 250 346______________________________________ .sup.(1) M = Monomer; TMSP MW = 112.19 C = Catalyst; TaCl5 MW = 357 M/C = Mole ratio of monomer to catalyst .sup.(2) Brookfield viscosity in toluene @ 1.7% TS in centipoise
Both flat sheet PTMSP membranes and PTMSP membranes coated on a porous hollow fiber substrate were fabricated by dissolving the polymer in toluene at a weight ratio of 1/40 to form a 2.5% solution by weight. A portion of the toluene-polymer solution was cast on a clean, smooth glass surface using a 40 mil. doctor knife, and air dried using a stream of dry nitrogen. The polymer film ranged from about 25-30 microns in total thickness. The flat sheet membranes were removed from the solid glass support by soaking in water. The films easily floated off of the glass surface. The flat sheet membranes were mounted in a CSC-135 Permeation Cell (manufactured by Custom Scientific Corporation, Whippany, NJ) using the procedure described in an article by S. A. Stern, et al. in Modern Plastics, October 1964.
The same toluene-polymer solution was used for coating CelgardŽ polypropylene porous hollow fiber using grade #X-20 of CelgardŽ material manufactured by Celanese Chemical Corporation. The CelgardŽ hollow fibers were dipped into the toluene-polymer solution twice to insure complete coverage of the outer surface of the fiber.
Several of the PTMSP membranes while still attached to the glass supports, were fluorinated in a gas phase batch reactor with various fluorine/nitrogen mixtures. The membranes were placed in the reactor and the gas space was purged for 4 hours with nitrogen to remove ambient air. Pre-set ratios of F2 /N2 were then flowed through the reactor space for predetermined periods of time.
Three PTMSP membranes were fluorinated for a period of five minutes using different fluorine gas concentrations. A study of the surface composition of the PTMSP membranes before and after fluorination indicates a drastic alteration in the surface of the membrane. The surface compositions of the three fluorinated membranes and one unflorinated PTMSP membrane were analyzed, and the results are reported in Table 2 below.
TABLE 2______________________________________ MEMBRANE Control 1 2 3______________________________________Fluorination TreatmentNitrogen (cc/min) 100 99.5 99.0 96.0Fluorine (cc/min) 0 0.5 1.0 4.0Element Atomic %Carbon 86.0 49.0 49.2 49.1Silicon 14.0 2.4 2.6 2.1Fluorine -- 27.4 27.0 30.2Oxygen -- 21.0 21.1 18.2______________________________________
The surface analysis reported in Table 2 shows a significant decrease in both the carbon and silicon contents on the surface of the fluorinated membranes. It is postulated that the reduction of silicon on the surface of the fluorinated polymeric membranes is due to the formation of volatile silicon compounds, such as SiF4 -, which are removed from the polymeric chain resulting in improved membrane selectivity.
Several other PTMSP membranes were synthesized and fluorinated in a gas phase batch reactor in accordance with the above procedures. The fluorine content of the treating gas stream ranged from 0.1-0.5% F2 with total F2 exposure ranging from 0.5-60 cc. Contact times of the membranes with the treating gas ranged from 1-60 min.
The fluorinated PTMSP membranes were recovered from the reactor and subsequently removed from the glass supports by a water wedge technique. The membranes were measured for total thickness and subsequently mounted in the CSC-135 Permeation Cells for gas permeability and selectivity studies.
Gas permeability and selectivity studies using the PTMSP membranes treated with various fluorine concentrations and contact times were carried out and are reported in the examples below. These examples are meant only to illustrate the present invention and are not meant to be limiting.
Two unfluorinated and nine fluorinated flat sheet PTMSP polymer membrane samples were mounted in separate CSC permeation cells such that pressurized gas mixtures could be passed over the membrane surface and the permeate stream could be measured on the permeate side of the membrane by a volumetric flow device.
The fluorinated samples differed in the fluorine concentration used as well as the contact time for fluorination. The permeability (P), permeance (P/L), and selectivity (α) of various gases through the membranes are reported in Tables 3 and 4 below.
TABLE 3__________________________________________________________________________Permeability and PermeanceMembrane # A B 1 2 3 4 5 6 7 8 9Thickness (cm) 141.0.sup.(1) 33.3.sup.(1) 98.63.sup.(1) 77.38.sup.(1) 105.5.sup.(1) 88.0.sup.(1) 134.63.sup.(1) 97.42.sup.(1) 152.3.sup.(1) 152.6.sup.(1) 141.3.sup.(1)__________________________________________________________________________Time (min) 5 1 7.5 1.5 5 15 60 60 60cc/N2 /min 100 100 200 200 100 800 200 400 200cc/F2 /min .1 0.5 0.2 1.0 0.5 0.8 0.2 0.4 1.0F2 % 0.1 0.5 0.1 0.5 0.5 0.1 0.1 0.1 0.5F2 (cc Total) 0.5 0.5 1.5 1.5 2.5 12 12 24 60--P.sup.(2) and --P/1.sup.(3)H2 ×10+10 16189 16110 12543 14075 10151 10115 9968 6176 8169 4476 4878 ×10+5 56.40 141.6 25.90 30.76 19.34 10.27 10.87 4.058 4.940He ×10+10 6756 6451 6052 6593 818 5876 6018 5122 5571 4915 4868 ×10+5 61.36 VL.sup.(4) 51.61 68.18 58.71 24.60 25.26 13.12 13.63O2 ×10+10 10228 9851 4333 4357 1963 1838 2374 967.8 1040 515.7 585.2 ×10+5 7.729 9.948 2.313 2.557 2.309 1.099 .7620 .3577 .4388N2 ×10+10 6765 6724 1348 1318 413.3 410.3 552.8 211.4 201 128 119.9 ×10+5 1.708 2.117 .4173 .4969 .4473 .2240 .1360 .08550 .08485CH4 ×10+10 15702 16296 1151 1283 196.3 261.4 311.5 115.3 90.4 97 44.7 ×10+5 1.167 1.803 .1884 .3020 .2314 .1192 .06969 .06400 .03172CO ×10+10 7752 7733 1767 1760 554 481.3 742.1 257.5 284.3 272.8 151.8 ×10+5 2.321 2.927 .5656 .5832 .6096 .2734 .1938 .1853 .1096CO2 ×10+10 32084 34114 20449 20449 20257 9559 9687 3718 3860 3563 2120 ×10+5 54.24 54.24 67.40 12.74 10.17 4.299 2.869 2.617 1.603__________________________________________________________________________ .sup.(1) ×10-4 .sup.(2) Permeability Coefficient for the Composite Membrane (×10+10) .sup.(3) Permeance of the fluorinated surface layer (×10+5) .sup.(4) Very large
TABLE 4__________________________________________________________________________SelectivityMembrane # A B 1 2 3 4 5 6 7 8 9Thickness (cm) 141.0.sup.(1) 33.3.sup.(1) 98.63.sup.(1) 77.38.sup.(1) 105.5.sup.(1) 88.0.sup.(1) 134.63.sup.(1) 97.42.sup.(1) 152.3.sup.(1) 152.6.sup.(1) 141.3__________________________________________________________________________Time (min) 5 1 7.5 1.5 5 15 60 60 60cc/N2 /min 100 100 200 200 100 800 200 400 200cc/F2 /min .1 0.5 0.2 1.0 0.5 0.8 0.2 0.4 1.0F2 % 0.1 0.5 0.1 0.5 0.5 0.1 0.1 0.1 0.5F2 (cc Total) 0.5 0.5 1.5 1.5 2.5 12.0 12.0 24.0 60.0αO2 /N2 ×10+10(2) 1.51 1.47 3.21 3.31 4.75 4.48 4.29 4.58 5.17 4.03 4.88 ×10+5(3) 4.53 4.70 5.54 5.15 5.16 4.91 5.60 4.18 5.18He/CH4 ×10+10 0.43 0.35 5.26 5.00 14.1 14.3 19.3 44.4 61.6 50.7 109 ×10+5 52.6 VL.sup.(4) 274 226 254 206 423 205 430H2 /CH4 ×10+10 1.03 0.99 10.9 10.7 24.6 24.7 32.0 53.6 90.4 46.1 109 ×10+5 48.3 78.5 137 102 83.6 86.2 182 63 156H2 /CO ×10+10 2.09 2.08 7.10 8.0 18.3 21.0 13.4 24.0 28.7 16.4 32.1 ×10+5 24.3 48.5 45.8 52.7 31.7 37.6 56.1 21.9 45.1CO2 /CH4 ×10+10 2.04 2.09 17.8 15.8 48.7 32.6 31.1 32.2 42.7 36.7 47.4 ×10+5 46.5 37.4 67.6 43.1 43.9 36.1 48.1 40.9 50.5CO2 /N2 ×10+10 4.74 5.07 15.2 15.4 23.1 20.7 17.5 17.6 19.2 27.8 17.7 ×10+5 31.8 31.8 30.5 26.2 22.7 19.2 21.1 30.6 18.9H2 /N2 ×10+10 2.39 2.40 9.30 10.7 25.6 24.7 18.0 29.2 40.6 35.0 40.7 ×10+5 33.0 66.9 62.1 61.9 43.2 45.8 79.9 47.5 52.9__________________________________________________________________________ .sup.(1) ×10-4 .sup.(2) Selectivity based on permeability coefficient (--P) of the composite membrane .sup.(3) Selectivity based on permeance (--P/1) of the fluorinated surface layer .sup.(4) Very large
The results reported in Tables 3 and 4 above for the gas permeability and selectivity tests, show a significant increase in membrane selectivity of the fluorinated membranes for all seven gas mixtures tested. For example, the O2 /N2 selectivity ratio of the PTMSP membrane showed over a two-fold increase for the membrane when fluorinated with 0.1% F2 gas for 5 minutes, and over a three-fold increase for the membrane when fluorinated with 0.1% F2 for 15 minutes. The largest selectivity increase was exhibited by the PTMSP membranes which were fluorinated with a 0.5% fluorine gas for 60 minutes, although a significant selectivity increase was observed even with the membranes which were fluorinated with only 0.1% fluorine gas. Table 3 also shows that PTMSP membranes, when fluorinated under the proper conditions, maintain good permeability characteristics while increasing selectivity.
The fluorination techniques used to treat the polytrimethyl silyl propyne polymers were also used to treat silicone rubber and poly 2-nonyne polymers.
Silicone rubber which is a crosslinked polymer having the general structural formula: ##STR9## when formed into a membrane has been shown to be very permeable for many gases yet exhibits relatively low selectivities. A 5 mil thick membrane of commercial silicone rubber (MEM-100, lot 190 B-163, manufactured by General Electric Comany) was fluorinated with a gas stream containing 0.5% F2 gas for 45 minutes. The permeabilities and selectivities for various gases were tested for both the fluorinated membrane and an unfluorinated membrane. Gas permeability values and surface analysis data for the fluorinated and unfluorinated membranes are reported in Table 5 below.
TABLE 5______________________________________Silicone Rubber Membranes Unfluorinated Fluorinated______________________________________--PHelium 300 291Oxygen 500 462Nitrogen 250 183Methane 800 523Surface Analysis by ESCA% C 50.8 53.4% O 27.3 19.4% Si 21.9 0.6% F -- 26.4______________________________________
The above permeability coefficient and surface analysis data indicate that the silicone rubber membrane is fluorinated, but that surface fluorination did not have a significant effect on permeability or selectivity of the membrane for the gases tested. Additionally, the fluorinated membrane eroded over time, making this polymer unsuitable for surface fluorination.
A sample of poly 2-nonyne was polymerized using a mixed MoCl5 /P(Ph)4 catalyst system. The resulting polymer, having the general structural formula: ##STR10## was formed into a dense membrane and treated with a F2 /N2 gas stream comprising 0.5% F2 gas for 15 minutes. Fluorinated and unfluorinated membrane samples were tested for permeability and selectivity for various gases, and a surface analysis was performed on both samples. The results of the tests and analyses are reported in Table 6 below.
TABLE 6______________________________________Poly 2-nonyne Membranes Unfluorinated Fluorinated______________________________________--POxygen 54.1 52.0Nitrogen 17.9 21.8Helium 70.3 62.0αO2 /N2 3.0 2.4He/N2 3.9 2.8He/O2 1.3 1.2Surface Analysis by ESCA% C 94.5 43.7% O 5.0 6.2% F -- 49.8______________________________________
The poly-2-nonyne membrane, when treated with an F2 /N2 reactive mixture, exhibited a highly fluorinated surface, but demonstrated no significant change in either permeability coefficient or selectivity for the gases tested.
The results of the above examples demonstrates the importance of both the basic polymer structure and the fluorination step in synthesizing a membrane having both high permeability and high selectivity for a wide range of gas mixtures.
Having this described the present invention, what is now deemed appropriate for Letters Patent is set out in the following appended claims.
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|EP0343556A3 *||May 22, 1989||Apr 3, 1991||Air Products And Chemicals, Inc.||Process for the polymerization of tri-substituted silylalkynes|
|EP0354514A2 *||Aug 7, 1989||Feb 14, 1990||Air Products And Chemicals, Inc.||Fluoro-oxidized polymeric membranes for gas separation and process for preparing them|
|EP0354514A3 *||Aug 7, 1989||Sep 26, 1990||Air Products And Chemicals, Inc.||Fluoro-oxidized polymeric membranes for gas separation and process for preparing them|
|WO1994009886A1 *||Nov 3, 1993||May 11, 1994||Membrane Technology And Research, Inc.||Gas-separation process|
|U.S. Classification||95/51, 427/248.1, 96/13, 96/10, 428/442, 95/55, 95/53, 96/12, 95/54|
|International Classification||C08F8/20, B01D67/00, C08J5/18, B01D53/22, B01D71/44, B01D71/70, C08F8/22|
|Cooperative Classification||B01D67/0093, C08F8/22, Y10T428/31649, B01D71/44|
|European Classification||B01D71/44, C08F8/22, B01D67/00R18|
|Dec 13, 1985||AS||Assignment|
Owner name: AIR PRODUCTS AND CHEMICALS, INC., P. O. BOX 538, A
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:LANGSAM, MICHAEL;REEL/FRAME:004496/0130
Effective date: 19851213
|Mar 27, 1990||CC||Certificate of correction|
|Jul 19, 1990||FPAY||Fee payment|
Year of fee payment: 4
|Nov 22, 1994||REMI||Maintenance fee reminder mailed|
|Apr 16, 1995||LAPS||Lapse for failure to pay maintenance fees|
|Jun 27, 1995||FP||Expired due to failure to pay maintenance fee|
Effective date: 19950419